Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Neda MOHAJER"'
Autor:
Saeed Talebi, Mona Entezam, Neda Mohajer, Golnaz-Ensieh Kazemi-sefat, Masoumeh Razipour, Somayeh Ahmadloo, Aria Setoodeh, Mohammad Keramatipour
Publikováno v:
Cell Journal, Vol 18, Iss 2, Pp 229-236 (2016)
Objective The phenylalanine hydroxylase (PAH) locus has high linkage disequilibrium. Haplotypes related to this locus may thus be considered sufficiently informative for genetic diagnosis and carrier screening using multi-allelic markers. In this
Externí odkaz:
https://doaj.org/article/03546ab4cd044946880c921e9ff48ca9
Autor:
Masoumeh RAZIPOUR, Daniz KOOSHAVAR, Elaheh ALAVINEJAD, Seyede Zahra SAJEDI, Neda MOHAJER, Aria SETOODEH, Saeed TALEBI, Mohammad KERAMATIPOUR
Publikováno v:
Iranian Journal of Public Health, Vol 46, Iss 4 (2017)
Phenylketonuria (PKU) is an inborn error of amino acid metabolism with an autosomal recessive inheritance caused in most cases by mutations in the phenylalanine hydroxylase (PAH) gene. PKU has wide allelic heterogeneity. Here we report a novel hetero
Externí odkaz:
https://doaj.org/article/1ac23fb6da4d43d3b79a4b0f179855cf
Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes
Autor:
Mohammad Keramatipour, Saeed Talebi, Seyede Zahra Sajedi, Golnaz-Ensieh Kazemi-sefat, Seyyed Mojtaba Mohaddes Ardebili, Masoumeh Razipour, Aria Setoodeh, Neda Mohajer, Jalal Gharesouran, Mona Entezam, Elaheh Alavinejad
Publikováno v:
Metabolic Brain Disease. 32:1685-1691
Phenylketonuria (PKU), one of the most common inborn errors of amino acid metabolism, is caused by mutations in the phenylalanine hydroxylase (PAH) gene (PAH). PKU has wide allelic heterogeneity, and over 600 different disease-causing mutations in PA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b402763adaaca7fb7a2b6220a12bb1b
https://doi.org/10.1007/s11011-017-0048-7
https://doi.org/10.1007/s11011-017-0048-7
Autor:
Elaheh, Alavinejad, Seyede Zahra, Sajedi, Masoumeh, Razipour, Mona, Entezam, Neda, Mohajer, Aria, Setoodeh, Saeed, Talebi, Mohammad, Keramatipour
Publikováno v:
Avicenna Journal of Medical Biotechnology
Background: Phenylalanine hydroxylase (PAH) gene is the well-known causative gene for classic Phenylketonuria (PKU) (OMIM#261600) disease, with more than 500 reported mutations. Through this study, a novel mutation in the PAH gene in an Iranian pedig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46164903227883123ff8dab203a92869
https://pubmed.ncbi.nlm.nih.gov/28706611
https://pubmed.ncbi.nlm.nih.gov/28706611
Autor:
Hodjatallah Rabbani, Mahmood Jeddi-Tehrani, Jalal Khoshnoodi, Fathollah Tahmasebi, Fazel Shokri, Tohid Kazemi, Neda Mohajer, Ali Ahmad Bayat
Publikováno v:
Hybridoma (2005). 30(4)
HER2 proto-oncogene encodes a transmembrane receptor tyrosine kinase overexpressed in a variety of solid tumors. Several mouse monoclonal antibodies (MAbs) have been developed that recognize the extracellular part of HER2; of them two MAbs were human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90415d45bae90848ac7772a209defce1
https://pubmed.ncbi.nlm.nih.gov/21851234
https://pubmed.ncbi.nlm.nih.gov/21851234
Publikováno v:
Physical Treatments, Vol 9, Iss 3, Pp 137-146 (2019)
Purpose: The present study investigated the most appropriate footprint index and its related parameters for the diagnosis of flatfoot, especially in cases with mild deformity. Methods: In total, 148 footprints were recorded from 77 young women with f
Externí odkaz:
https://doaj.org/article/26817a415a0e491b8d46fdfdb6a9a85d
Publikováno v:
Advances in High Energy Physics, Vol 2018 (2018)
Since the doubly heavy baryons masses are experimentally unknown (except Ξcc+ and Ξcc++), we present the ground state masses and the positive and negative parity excited state masses of doubly heavy Ξ baryons. For this purpose, we have solved the
Externí odkaz:
https://doaj.org/article/786115acd08a4193933dc4d6b3dcf132